RESUMO
Undifferentiated type A spermatogonia are the foundation of fish spermatogenesis. This cell population includes the spermatogonial stem cell population, which is able to either self-renew or differentiate into cells that will generate the male gamete - the spermatozoa. Spermatogonia stem cells are located in a specific region of the testes known as the spermatogonial niche, which regulates spermatogonial stem cell function. This study characterizes undifferentiated type A spermatogonia and their S-phase label-retaining cell properties in Astyanax altiparanae testes. This is a fish species of substantial commercial, environmental, and academic importance. Two types of undifferentiated spermatogonia have been described in A. altiparanae testis: Aund* and Aund. Among the main differences observed, Aund* spermatogonia have an irregular nuclear envelope, decondensed chromatin, one or two nucleoli, and nuages in the cytoplasm; meanwhile, type Aund have a round nucleus. Aund* is preferentially distributed in areas neighboring the interstitial compartment, whereas Aund is located in the intertubular area. Finally, this study found that undifferentiated type A spermatogonia were able to retain BrdU over a long chase period, suggesting that these cells have a long cell cycle and potential stem cell candidates among them. Based on these findings, undifferentiated type A spermatogonia may be characterized as putative stem cells in A. altiparanae testis. This work will contribute to further studies on the stem cell biology of this promising Neotropical experimental model.
Assuntos
Diferenciação Celular/fisiologia , Peixes/fisiologia , Espermatogônias/fisiologia , Animais , Masculino , Células-Tronco/fisiologiaRESUMO
Similar to mammals, spermatogenesis in fish is initiated by spermatogonial stem cells (SSCs) which either self-renew or gradually differentiate to produce mature sperm. SSCs are located in a particular testis microenvironment called SSC ni che, formed by Sertoli and peritubular myoid cells, the basement membrane and other cellular components/factors from the intertubular compartment that regulate SSCs maintenance and fate. Considering the great variation in testis structure/arrangemen t across fish species, the study of the niche components is crucial to understand SSCs physiology. Additionally, the germ cell transplantation technique, which has been applied to fish in the last decade, is a unique approach to elucidating important functional aspects of SSCs biology such as: (i) the capacity of SSCs to colonize the testis of recipient species (syngeneic and xenogeneic transplantation) giving rise to donor sperm; (ii) the plasticity of these cells, considering that spermatogonia and oogonia can be derived from SSCs collected from the opposite sex; and (iii) the possibility of genetically manipulating SSCs before transplantation to produce transgenic fish. However, fish SSC isolation and characterization has been lim ited so far by the lack of specific molecular markers fo r these cells. Therefore, various research groups are currently investigating specific SSCs markers and, up to date, few proteins have been identified in different spermatogonial populations from distinct fish species (e.g. Notch1, Ly75, Plzf, Oct-4, SGSA -1). Furthermore, the development of a fish SSC culture system would allow the investigation of important regulatory aspects of the SSC physiology in well-defined conditions as well as to in vitro amplify these rare cells. Overall, the study of SSC physiology, niche and transplantation in fish has opened up new scenarios for the development of aquaculture and reproductive biotechnologies such as germplasm conservation of endangered or commercially important species and the possibility of generating transgenic fish.(AU)
Assuntos
Animais , Espermatogênese/fisiologia , Espermatozoides/citologia , Fisiologia , Aquicultura/tendências , Peixes/classificação , Biotecnologia/métodosRESUMO
Similar to mammals, spermatogenesis in fish is initiated by spermatogonial stem cells (SSCs) which either self-renew or gradually differentiate to produce mature sperm. SSCs are located in a particular testis microenvironment called SSC ni che, formed by Sertoli and peritubular myoid cells, the basement membrane and other cellular components/factors from the intertubular compartment that regulate SSCs maintenance and fate. Considering the great variation in testis structure/arrangemen t across fish species, the study of the niche components is crucial to understand SSCs physiology. Additionally, the germ cell transplantation technique, which has been applied to fish in the last decade, is a unique approach to elucidating important functional aspects of SSCs biology such as: (i) the capacity of SSCs to colonize the testis of recipient species (syngeneic and xenogeneic transplantation) giving rise to donor sperm; (ii) the plasticity of these cells, considering that spermatogonia and oogonia can be derived from SSCs collected from the opposite sex; and (iii) the possibility of genetically manipulating SSCs before transplantation to produce transgenic fish. However, fish SSC isolation and characterization has been lim ited so far by the lack of specific molecular markers fo r these cells. Therefore, various research groups are currently investigating specific SSCs markers and, up to date, few proteins have been identified in different spermatogonial populations from distinct fish species (e.g. Notch1, Ly75, Plzf, Oct-4, SGSA -1). Furthermore, the development of a fish SSC culture system would allow the investigation of important regulatory aspects of the SSC physiology in well-defined conditions as well as to in vitro amplify these rare cells. Overall, the study of SSC physiology, niche and transplantation in fish has opened up new scenarios for the development of aquaculture and reproductive biotechnologies such as germplasm conservation of endangered or commercially important species and the possibility of generating transgenic fish.